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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183878Generated: November 1, 2026

Sodium triacetoxyborohydride → Imidazo[1,2-a]pyrimidin-7-ylmethanol

https://huagongshe.com/reaction/2183878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantImidazo[1,2-A]pyrimidine-7-carbaldehydeHCID 18001283—
SolventMethanolHCID 887—
ProductImidazo[1,2-a]pyrimidin-7-ylmethanolHCID 1800129399.8%

Reaction Steps

Sodium triacetoxyborohydride (21.5 g, 102 mmol) was added portionwise over 20 min to a stirred solution of imidazo[1,2-α]pyrimidine-7-carbaldehyde (5.00 g, 34.0 mmol) in methanol (100 ml) and the solution left to stir at ambient temperature for 18 h. The solvent was evaporated, the residue redissolved in methanol (150 ml) and pre-adsorbed onto silica. Purification by chromatography on silica gel eluting with dichloromethane (containing 1% conc. ammonia) on a gradient of methanol (1-10%) gave imidazo[1,2-α]pyrimidin-7-ylmethanol (5.06 g, 99%) as a white solid: δH (360 MHz, DMSO) 4.57 (2H, d, J 6), 5.62 (1H, t, J 6), 7.13 (1H, d, J 7), 7.64 (1H, d, J 1), 7.86 (1H, d, J 1), 8.94 (1H, d, J 7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900215B2
Source datasetuspto-grants-2005_05
ORD IDord-54c683e473924bf4a7a66fab3872d54c
Source noteuspto-grants-2005_05